5-Butyl-3-phenyl-4,5-dihydroisoxazole

Base Information

Chemical Name:5-Butyl-3-phenyl-4,5-dihydroisoxazole
CAS No.:1017-09-0
Molecular Formula:C13H17NO
Molecular Weight:203.284
Hs Code.:
DSSTox Substance ID:DTXSID80456586
Nikkaji Number:J565.157C
Mol file:1017-09-0.mol

Synonyms:5-butyl-3-phenyl-4,5-dihydroisoxazole;1017-09-0;Isoxazole, 5-butyl-4,5-dihydro-3-phenyl-;SCHEMBL10411521;3-Phenyl-5-butyl-2-isoxazoline;DTXSID80456586;5-butyl-3-phenyl-4,5-dihydro-isoxazole

Suppliers and Price of 5-Butyl-3-phenyl-4,5-dihydroisoxazole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 5-Butyl-3-phenyl-4,5-dihydroisoxazole

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:203.131014166
Heavy Atom Count:15
Complexity:219

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC1CC(=NO1)C2=CC=CC=C2

Technology Process of 5-Butyl-3-phenyl-4,5-dihydroisoxazole

There total 12 articles about 5-Butyl-3-phenyl-4,5-dihydroisoxazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 592-41-6,25067-06-5
1-hexene

: 5585-14-8
3,4-diphenyl-furazan 2-oxide

: 1017-09-0
5-n-butyl-3-phenyl-Δ²-isoxazoline

Guidance literature:: 3,4-diphenyl-furazan 2-oxide; Flash vacuum pyrolysis;

1-hexene; In diethyl ether; Inert atmosphere;
DOI:10.3998/ark.5550190.0011.a04

Reference yield: 90.0%

: 698-16-8
benzohydroximoyl chloride

: 126688-97-9
2-[(1E)-hex-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 1017-09-0
5-n-butyl-3-phenyl-Δ²-isoxazoline

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 3h; Reagent/catalyst; regioselective reaction;
DOI:10.1002/jhet.2667